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1
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0002634798
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For excellent reviews, see:. Ojima I. (Ed), Wiley-VCH, New York
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For excellent reviews, see:. Ohkuma T., Kitamura M., and Noyori R. In: Ojima I. (Ed). Catalytic Asymmetric Synthesis (2000), Wiley-VCH, New York 1-110
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(2000)
Catalytic Asymmetric Synthesis
, pp. 1-110
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Ohkuma, T.1
Kitamura, M.2
Noyori, R.3
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12
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10744227163
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Burk M.J., de Koning P.D., Grote T.M., Hoekstra M.S., Hoge G., Jennings R.A., Kissel W.S., Le T.V., Lennon I.C., Mulhern T.A., Ramsden J.A., and Wade R.A. J. Org. Chem. 68 (2003) 5731
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(2003)
J. Org. Chem.
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Burk, M.J.1
de Koning, P.D.2
Grote, T.M.3
Hoekstra, M.S.4
Hoge, G.5
Jennings, R.A.6
Kissel, W.S.7
Le, T.V.8
Lennon, I.C.9
Mulhern, T.A.10
Ramsden, J.A.11
Wade, R.A.12
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13
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0035911373
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Saylik D., Campi E.M., Donohue A.C., Jackson W.R., and Robinson A.J. Tetrahedron: Asymmetry 12 (2001) 657
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(2001)
Tetrahedron: Asymmetry
, vol.12
, pp. 657
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Saylik, D.1
Campi, E.M.2
Donohue, A.C.3
Jackson, W.R.4
Robinson, A.J.5
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18
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33845281011
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For detailed mechanistic studies of this reaction, see:
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For detailed mechanistic studies of this reaction, see:. Landis C.R., and Halpern J. J. Am. Chem. Soc. 109 (1987) 1746
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(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 1746
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Landis, C.R.1
Halpern, J.2
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20
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0025766920
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For efficient preparation of Ru-BINAP catalysts, see:
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For efficient preparation of Ru-BINAP catalysts, see:. Kitamura M., Tokunaga M., Ohkuma T., and Noyori R. Tetrahedron Lett. 32 (1991) 4163
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(1991)
Tetrahedron Lett.
, vol.32
, pp. 4163
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Kitamura, M.1
Tokunaga, M.2
Ohkuma, T.3
Noyori, R.4
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21
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0001317451
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Takaya H., Ohta T., Inoue S.-i., Tokunaga M., Kitamura M., and Noyori R. Org. Synth. 72 (1994) 74
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(1994)
Org. Synth.
, vol.72
, pp. 74
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Takaya, H.1
Ohta, T.2
Inoue, S.-i.3
Tokunaga, M.4
Kitamura, M.5
Noyori, R.6
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22
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0001156975
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Benincori T., Brenna E., Sannicolò F., Trimarco L., Antognazza P., Cesarotti E., Demartin F., and Pilati T. J. Org. Chem. 61 (1996) 6244
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J. Org. Chem.
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Benincori, T.1
Brenna, E.2
Sannicolò, F.3
Trimarco, L.4
Antognazza, P.5
Cesarotti, E.6
Demartin, F.7
Pilati, T.8
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25
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28044454135
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For recent discussions of electronic effects in asymmetric hydrogenations, see:
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For recent discussions of electronic effects in asymmetric hydrogenations, see:. Dubrovina N.V., Tararov V.I., Monsees A., Spannenberg A., Kostas I.D., and Börner A. Tetrahedron: Asymmetry 16 (2005) 3640
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(2005)
Tetrahedron: Asymmetry
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Dubrovina, N.V.1
Tararov, V.I.2
Monsees, A.3
Spannenberg, A.4
Kostas, I.D.5
Börner, A.6
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26
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0347761350
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Jeulin S., de Paule S.B., Ratovelomanana-Vidal V., Genet J.P., Champion N., and Dellis P. Angew. Chem., Int. Ed. 43 (2004) 320
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(2004)
Angew. Chem., Int. Ed.
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Jeulin, S.1
de Paule, S.B.2
Ratovelomanana-Vidal, V.3
Genet, J.P.4
Champion, N.5
Dellis, P.6
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27
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33646116499
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Jones, Z. A.; Ph.D. Dissertation, University of Cambridge, 2005.
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33646078273
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note
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The formation of stable seven-membered chelate rings of the ruthenium catalyst and the Z-isomer cannot be ruled out as it was observed that ruthenium(II) in these solutions was considerably less sensitive to oxygen than the corresponding systems containing the E-isomer.
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29
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33751155033
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Ohta T., Miyake T., Seido N., Kumobayashi H., and Takaya H. J. Org. Chem. 60 (1995) 357
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(1995)
J. Org. Chem.
, vol.60
, pp. 357
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Ohta, T.1
Miyake, T.2
Seido, N.3
Kumobayashi, H.4
Takaya, H.5
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30
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33646113795
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note
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Using pyridine as a stoichiometric or catalytic additive did not increase conversion with unreactive substrates. Therefore, pyridine substituents most likely serve as coordination sites.
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31
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33646119813
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note
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3).
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32
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0347745231
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4 to the corresponding amine (80%, no racemization observed), being previously described in enantiomerically pure form:
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4 to the corresponding amine (80%, no racemization observed), being previously described in enantiomerically pure form:. Zabel M., Breu J., Rau F., Range K.-J., Krey A., Uffrecht A., and Buschauer A. Acta Cryst. C56 (2000) 250
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(2000)
Acta Cryst.
, vol.C56
, pp. 250
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Zabel, M.1
Breu, J.2
Rau, F.3
Range, K.-J.4
Krey, A.5
Uffrecht, A.6
Buschauer, A.7
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33
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0034988181
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The configuration of all other products was assigned in analogy to these results
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Schuster A., Götte C., Bernhardt G., and Buschauer A. Chirality 13 (2001) 285 The configuration of all other products was assigned in analogy to these results
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(2001)
Chirality
, vol.13
, pp. 285
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Schuster, A.1
Götte, C.2
Bernhardt, G.3
Buschauer, A.4
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